Literature DB >> 4855265

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

P E Podruch, B Weisskopf.   

Abstract

Mesh：

Year:  1974        PMID： 4855265     DOI： 10.1016/s0022-3476(74)80296-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  14 in total

1.  Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.

Authors:  U Francke; C Kernahan; C Bradshaw
Journal:  Humangenetik       Date:  1975

2.  A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).

Authors:  M K Mason; D A Spencer; A Rutter
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

3.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

4.  Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975-12-23

5.  A case of trisomy for the short arm of chromosome no. 9(+9(p)).

Authors:  M E Käosaar; A V Mikelsaar; T A Talvik; R V Mikelsaar
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

6.  Trisomy 9p resulting from maternal 9/21 translocation.

Authors:  I Sŭbrt; B Blehová; B Pallová
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

7.  47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Authors:  H Fujita; M Shimazaki; T Takeuchi; Y Hayakawa; T Oura
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

Review 8.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

9.  Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Authors:  M Tolksdorf; J Kunze; G Gross-Selbeck; K Sperling; R D Wegner; V Wieczorek; M Vogel
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

Review 10.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
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